Hydroxyzine hydrochloride

Product NDC

66267-792

11-digit product format

662670792

Labeler code

66267

Product ID

66267-792_46dbb362-01a4-1e3e-e054-00144ff88e88

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Hydroxyzine hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

NuCare Pharmaceuticals, Inc.

Application

ANDA204279

Marketing category

ANDA

Marketing start

2012-03-24

Marketing end

0000-00-00

Substance

HYDROXYZINE HYDROCHLORIDE

Active strength

25 mg/1

Pharmacologic classes

Antihistamine [EPC],Histamine Receptor Antagonists [MoA]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record